Síndrome de Barth en la edad adulta: un caso clínico-Reference-Cited by-同舟云学术

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Síndrome de Barth en la edad adulta: un caso clínico

Published:2013-01 Issue:1 Volume:66 Page:68-70
ISSN:0300-8932
Container-title:Revista Española de Cardiología
language:es
Short-container-title:Revista Española de Cardiología

Author:

Sabater-Molina María,Guillén-Navarro Encarna,García-Molina Esperanza,Ballesta-Martínez María Juliana,Escudero Fuensanta,Ruiz-Espejo Francisco

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference6 articles.

1. Dilated cardiomyopathy;Jefferies;Lancet,2010

2. Clinical and genetic issues in dilated cardiomyopathy: A review for genetics professionals;Hershberger;Genet Med,2010

3. A novel X-linked gene, G4. 5. is responsible for Barth syndrome;Bione;Nat Genet,1996

4. Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth;Steward;Prenat Diagn,2010

5. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria;Kelley;J Pediatr,1991

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1. Inward rectifier potassium (Kir) channels in the retina: living our vision;American Journal of Physiology-Cell Physiology;2022-09-01

2. Barth syndrome: cardiolipin, cellular pathophysiology, management, and novel therapeutic targets;Molecular and Cellular Biochemistry;2021-01-07

3. TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome;Gene;2020-02

4. Neuromuscular Disorders;Self-Assessment Questions for Clinical Molecular Genetics;2019

5. PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases;Orphanet Journal of Rare Diseases;2018-01-25

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